| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48944758-48944850 | Rare:35 | ||||
| chr17:49210175-49210432 | Common:2; Rare:39 | ||||
| chr17:49210591-49210718 | Rare:20 | ||||
| chr17:49414833-49415120 | Common:1; Rare:68 | ||||
| chr17:49677961-49678193 | Rare:61 | ||||
| chr17:49788557-49788750 | Common:1; Rare:64 | ||||
| chr17:50186393-50186685 | Common:2; Rare:70; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr17:50188901-50189172 | Rare:72; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:50345926-50346136 | Common:4; Rare:69 | ||||
| chr17:50373157-50373221 | Common:2; Rare:30 | ||||
| chr17:50397405-50397633 | Common:1; Rare:67 | ||||
| chr17:50426090-50426252 | Common:1; Rare:40 | ||||
| chr17:50508191-50508457 | Common:4; Rare:77 | ||||
| chr17:50707972-50708116 | Rare:25 | ||||
| chr17:50719463-50719760 | Rare:112 |